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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:0081020 | congenital fibrosis of the extraocular muscles 5 | HGNC:18603 | Homo sapiens (human) | 84570 | COL25A1 |
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| DOID:0081111 | osteosclerotic metaphyseal dysplasia | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:14330 | Parkinson's disease | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:0060371 | Parkinson's disease 8 | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:13533 | osteopetrosis | HGNC:18608 | Homo sapiens (human) | 79705 | LRRK1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:0050890 | synucleinopathy | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:0060371 | Parkinson's disease 8 | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:8778 | Crohn's disease | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:7148 | rheumatoid arthritis | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:0080855 | Parkinsonism | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:14330 | Parkinson's disease | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:1289 | neurodegenerative disease | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:9743 | diabetic neuropathy | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:9255 | frontotemporal dementia | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:162 | cancer | HGNC:18618 | Homo sapiens (human) | 120892 | LRRK2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0070262 | congenital disorder of glycosylation type IIj | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0070257 | congenital disorder of glycosylation type IIe | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:630 | genetic disease | HGNC:18622 | Homo sapiens (human) | 91949 | COG7 |
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| DOID:0070260 | congenital disorder of glycosylation type IIh | HGNC:18623 | Homo sapiens (human) | 84342 | COG8 |
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